EP1303294B1 - Verfahren zur behandlung von instabiler angina pectoris - Google Patents

Verfahren zur behandlung von instabiler angina pectoris Download PDF

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Publication number
EP1303294B1
EP1303294B1 EP01960527A EP01960527A EP1303294B1 EP 1303294 B1 EP1303294 B1 EP 1303294B1 EP 01960527 A EP01960527 A EP 01960527A EP 01960527 A EP01960527 A EP 01960527A EP 1303294 B1 EP1303294 B1 EP 1303294B1
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EP
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Prior art keywords
rhdl
use according
infusion
apolipoprotein
administered
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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EP01960527A
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German (de)
English (en)
French (fr)
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EP1303294A2 (de
Inventor
Thomas F. LÜSCHER
Georg Noll
Peter Lerch
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CSL Behring AG
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ZLB Bioplasma AG
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • the invention relates to the use of reconstituted HDL for the improvement of endothelial function in hypercholesterolemia and for the therapy or prophylaxis of acute coronary diseases such as unstable angina or myocardial infarction.
  • the endothelium separates the blood from the extravascular tissue and on the other hand regulates important functions of the vessel wall.
  • An important prerequisite for the full function of the endothelial monolayer is its functional and structural integrity.
  • Some of the important functions of the endothelium are the control of the adhesion of cells (monocytes, platelets), the invasion of immunocompetent cells and the proliferation of smooth muscle cells.
  • biologically active substances are produced in the endothelial cells, such as prostaglandins, nitric oxide (NO) or endothelin-1. These substances affect the structure, metabolism and permeability of vessels, modulate vascular tone and control coagulation, fibrinolysis and inflammatory responses.
  • Endothelial injury or inflammation leads to malfunction, a critical factor in the development of atherosclerosis. This process can take years or decades to complete, leading to no clinical symptoms at an early stage. However, structural changes in the vascular wall can be detected by appropriate methods at this stage. High cholesterol levels, especially high LDL cholesterol or low HDL cholesterol favors the rapid development of atherosclerosis, which is usually associated with fatty deposits Streaks begins, which can later develop into plaques. Such plaques can locally lead to reduced blood flow, or even rupture under increased mechanical stress, thrombi and lead to acute coronary syndromes such as unstable angina or myocardial infarction. The unstable angina pectoris is also described as an inflammatory reaction, which leads to a systematic malfunction of the endothelial cells.
  • the therapy of the acute coronary syndromes tries to restore or replace the inadequate function of the endothelial cells. That is, it is aimed at a coronary vasodilation, an inhibition of platelets, an inhibition of coagulation or revascularization (bypass, PTCA / stenting).
  • the pharmaceutical agents used are GP IIb-IIIa antagonists, heparin, Cox inhibitors or NSAIDs (aspirin), betablockers and nitrates.
  • NSAIDs aspirin
  • betablockers betablockers
  • HDL cholesterol level As already mentioned, a risk factor that can lead to atherosclerosis or acute coronary syndromes is a decreased HDL cholesterol level. It is suspected that HDL leads with the so-called reverse cholesterol transport superfluous cholesterol from the periphery into the liver, there cholesterol is processed to bile acids and then excreted via bile. At low plasma HDL concentrations, cholesterol is eliminated too slowly and can deposit in vessel walls.
  • the endothelial function can be measured in vivo by various methods. Coronary circulation can be quantified with catheterization and new imaging techniques. Better and easier to access is the measurement of circulation in the forearm. Although in In these vessels, no lesions are normally observed, even slight changes in vascular functions can be observed with this method. With plethysmography, small changes in blood flow can be determined on stimulation with acetylcholine. With new, non-invasive ultrasound systems, the diameter of arteries can be accurately determined, allowing the vascular function to be checked and assessed.
  • Reconstituted HDL can be obtained from plasma, apolipoprotein A-1 and soybean lecithin.
  • Methods for obtaining reconstituted HDL are described, for example, in Circulatory Shock 40 (1993), 14-23, or in U.S. Patents 5,089,602, 5,128,318, and 5,652,339.
  • rHDL binds to lipids or lipid-like substances, such as lipopolysaccharides of Gram-negative bacteria in the blood and can thus be used for the treatment of septic shock.
  • rHDL was administered to patients with elevated plasma cholesterol levels and thus an increased risk of acute coronary syndromes such as unstable angina pectoris or myocardial infarction.
  • acute coronary syndromes such as unstable angina pectoris or myocardial infarction.
  • patients underwent endothelial function in forearm circulation. It was surprisingly found that a very rapid, acute improvement of a previously impaired endothelial function after infusion of rHDL can be achieved. This observed acute effect of rHDL is unexpected and can not be explained or compatible with today's understanding of the biological effects of rHDL in reverse cholesterol transport.
  • an infusion of rHDL can not reverse the effects of atherosclerosis, such as fatty streaks or plaques, built up over decades over a short period of just a few hours. Rather, it is believed that it is a hitherto unknown, acute systemic effect, which can very quickly improve the impaired function of the endothelial cells and thus for the treatment and / or prophylaxis of coronary diseases, especially unstable angina or myocardial infarction, can be used.
  • rHDL is a body-like substance, so the treatment is largely without side effects.
  • the effect of rHDL is believed to be due to improved bioavailability of NO in the vascular wall, which leads to inhibition of platelet adhesion and aggregation and relaxes the vascular tone.
  • patients with acute coronary disease such as unstable angina pectoris, may experience a lower incidence of secondary complications.
  • Unstable angina pectoris is a clinical syndrome of myocardial ischemia characterized by pectanginal chest pain at rest with ECG changes. Myocardial infarction is differentiated by biochemical markers of myocardial injury (CK, CK-MB) and ECG.
  • An object of the present invention is thus the use of reconstituted HDL for the preparation of an agent for improving endothelial function, in particular an agent for improving acute endothelial function in vascular diseases, e.g. the acute function of the coronary endothelium, especially in human medicine.
  • Another object of the invention is the use of reconstituted HDL for the preparation of an agent for the prophylaxis and / or treatment of acute coronary diseases such as unstable angina or myocardial infarction.
  • rHDL can be used, for example, in diseases such as non-Q-wave infarction and acute coronary diseases without, with a slightly elevated and strongly elevated troponin T levels are used.
  • Particularly preferred rHDL is used to improve the endothelium-dependent vasodilation in human patients.
  • rHDL is conveniently by infusion, e.g. by arterial, intraperitoneal or preferably intravenous infusion at a dosage of 10 to 150 mg, preferably 40 to 80 mg per kg of body weight per treatment.
  • the dose administered may be e.g. in an amount of 20 to 100 mg, especially 20 to 80 mg rHDL corresponding to 0.04 to 0.6 mg rHDL per min (dose based on protein) for a period of 10 minutes to several hours infused. If necessary, the rHDL infusion may be repeated one or more times if necessary.
  • the administered rHDL contains apolipoprotein A-1 and phospholipid, e.g. Phosphatidylcholine, preferably in a molar ratio of 1:50 to 1: 250, more preferably in a ratio of about 1: 150 and may additionally contain other lipids such as cholesterol, preferably up to a molar ratio of 1:20, e.g. 1: 5 to 1:20 (versus the apolipoprotein).
  • phospholipid e.g. Phosphatidylcholine
  • RHDL administration may be accompanied by the administration of other therapeutic agents such as GP IIb-IIIa antagonists, e.g. Antibodies such as RheoPro, integrilin or tirofiban, heparin, COX inhibitors or NSAIDs such as aspirin, beta-blockers or nitrates. Particularly preferred is a combined administration with heparin or / and aspirin.
  • GP IIb-IIIa antagonists e.g. Antibodies such as RheoPro, integrilin or tirofiban, heparin, COX inhibitors or NSAIDs such as aspirin, beta-blockers or nitrates.
  • the invention relates to the use for the prophylaxis and / or treatment of acute coronary disorders or coronary syndromes, such as unstable angina pectoris or myocardial infarction, wherein rHDL is administered.
  • the administration takes place to a subject, preferably a human patient, in such a way that it becomes more acute for relief or elimination Coronary syndrome sufficient amount of rHDL in a suitable form, for example by infusion is administered.
  • the forearm blood flow was simultaneously determined in both arms by venous occlusion plethysmography (EC-4, Hokanson) (Benjamin et al, Hypertension 25 (1995), 918-923). The subjects were stretched out with slightly raised arms above the level of the heart to improve venous drainage. Hand circulation was prevented by wrist supraystolic pressure bandages (220 mmHg) one minute prior to measurements (Kerslake, J. Physiol. 108 (1949), 451-457).
  • acetylcholine (Miochol E, Ciba Vision, Switzerland) and sodium nitroprusside (Nipruss, Schwarz Pharma, Germany) were added to the brachial artery in increasing amounts of 0.15, 0.45, 1.5, 4, 5 and 15 ⁇ g x 100 ml forearm volume (FAV) -1 x min -1 (each in 0.9% NaCl for 5 minutes) and 1.3 and 10 ⁇ g x 100 ml FAV -1 x min -1 (in 5% Glucose for 3 minutes) at a constant rate through an infusion pump via a catheter inserted under local anesthesia.
  • FAV forearm volume
  • the results are expressed as means ⁇ standard deviation (SD).
  • SD standard deviation
  • the mean values for forearm blood flow were obtained from at least three consecutive records during the last minute of the drug infusion. They are expressed as the percentage of infused to non-infused arm to account for changes in the bloodstream caused by systemic factors.
  • Plethysmographic measurements were compared using two-way ANOVA for repeated measurements (Wallenstein and Zucker, Circ.Res. 47 (1980), 1-9).
  • Clinical data were compared using the paired or unpaired Student T test (StatView 4.5, Abacus Concept). Statistical significance was assumed to be P ⁇ 0.05.
  • the clinical characteristics of the participants in the study are shown in Table 1.
  • the hypercholesterolemic and normocholesterolemic study groups differed only in lipid concentrations and body mass index. There was no difference in basal forearm blood flow in the two groups.
  • FBF means forearm blood flow
  • the forearm blood flow is simultaneously determined on both arms by venous occlusion plethysmography.
  • a blood pressure cuff inflated to 40 mm Hg, venous blood flow to the upper arm is prevented, so that only blood can flow into the arm - but not out.
  • the resulting increase in forearm circumference is measured with a stretch-sensitive rubber band.
  • Hand circulation is temporarily interrupted with a wrist cuff. The signal recording is carried out as described in Example 1.
  • acetylcholine or sodium nitroprusside as described in Example 1, infused.
  • positron emission tomography PET
  • GE Advance PET Tomograph GE Medical Systems, Milwaukee, Wisconsin
  • the volunteers are given 700-900 MBq 13 N ammonia or 15 O water in a peripheral vein by bolus injection while serial transaxial tomographic images of the heart are recorded (frame: 12 x 10 s, 4 x 30 s, 1 x 60 s and 2 x 30 s).
  • a 20 minute transmission scan for photon attenuation correction is performed using external 68 Ge sources.
  • the myocardial blood flow (MBF) is measured at rest and under standard stress conditions, ie administration of adenosine (0, 14 mg / kg / min for 7 minutes).
  • the heart is divided into 16 segments according to the recommendations of the American Society of Echocardiography.
  • the left ventricular bloodstream is examined.
  • the MBF is based on a Muzik et al. (J. Nucl. Med. 34 (1993), 83-91) and according to Hutchins (J. Am. Coll. Cardiol. 15 (1990), 1032-1042) and Hutchins et al. (J. Nucl. Med. 33 (1992), 1243-1250).
  • the coronary flow reserve (CFR) is calculated as the ratio between hyperemic and resting MBF values. The reproducibility of this method is described by Kaufmann et al. (J. Nucl. Med. 40 (1999), 1848-1856) and Wyss et al. (Eur. Heart J. 21 (2000), 568).
  • rHDL is infused intravenously over a period of 4 hours at a dosage of 80 mg / kg and the endothelial function is measured a second time. Blood pressure and heart rate are recorded continuously.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
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  • Animal Behavior & Ethology (AREA)
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EP01960527A 2000-07-20 2001-07-20 Verfahren zur behandlung von instabiler angina pectoris Expired - Lifetime EP1303294B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10035352 2000-07-20
DE10035352A DE10035352A1 (de) 2000-07-20 2000-07-20 Verfahren zur Behandlung von instabiler Angina pectoris
PCT/EP2001/008425 WO2002007753A2 (de) 2000-07-20 2001-07-20 Verfahren zur behandlung von instabiler angina pectoris

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EP1303294A2 EP1303294A2 (de) 2003-04-23
EP1303294B1 true EP1303294B1 (de) 2006-07-26

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EP01960527A Expired - Lifetime EP1303294B1 (de) 2000-07-20 2001-07-20 Verfahren zur behandlung von instabiler angina pectoris

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US (1) US7053049B2 (pl)
EP (1) EP1303294B1 (pl)
JP (1) JP4928047B2 (pl)
KR (2) KR20070108955A (pl)
AT (1) ATE333887T1 (pl)
AU (2) AU8200401A (pl)
CA (1) CA2418238C (pl)
DE (2) DE10035352A1 (pl)
DK (1) DK1303294T3 (pl)
ES (1) ES2266234T3 (pl)
HU (1) HU230151B1 (pl)
IL (2) IL154006A0 (pl)
NO (1) NO329848B1 (pl)
NZ (1) NZ523784A (pl)
PL (1) PL204406B1 (pl)
WO (1) WO2002007753A2 (pl)
ZA (1) ZA200300509B (pl)

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WO2007000924A1 (ja) * 2005-06-28 2007-01-04 Osaka University プログラニュリン活性を抑制または促進する物質を含む医薬組成物、およびプログラニュリン活性を抑制または促進する物質のスクリーニング方法
US7956035B2 (en) * 2007-03-01 2011-06-07 Csl Limited Treatment of endothelial dysfunction in diabetic patients
US20090110739A1 (en) * 2007-05-15 2009-04-30 University Of North Texas Health Science Center At Forth Worth Targeted cancer chemotherapy using synthetic nanoparticles
CA2780482A1 (en) 2008-11-17 2010-05-10 Anil K. Sood Hdl particles for delivery of nucleic acids
CN104487253B (zh) 2012-09-25 2016-05-25 惠普发展公司，有限责任合伙企业 液滴检测
ITMI20131300A1 (it) * 2013-08-01 2015-02-02 Nobil Bio Ricerche Srl Composizione per il riempimento di difetti ossei e parodontali
US9763892B2 (en) 2015-06-01 2017-09-19 Autotelic Llc Immediate release phospholipid-coated therapeutic agent nanoparticles and related methods
GB2603950A (en) 2021-02-22 2022-08-24 Reckitt & Colman Overseas Hygiene Home Ltd Effervescent germicidal compositions

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US5128318A (en) * 1987-05-20 1992-07-07 The Rogosin Institute Reconstituted HDL particles and uses thereof
CA1335077C (en) * 1988-02-08 1995-04-04 Henri Isliker Process for the manufacture of apolipoproteins from human blood plasma or serum
EP0543417A1 (en) * 1991-11-22 1993-05-26 Lipogenics, Incorporated Tocotrienols and tocotrienol-like compounds and methods for their use
US5652339A (en) * 1993-12-31 1997-07-29 Rotkreuzstiftung Zentrallaboratorium Method of producing reconstituted lipoproteins
JPH10218861A (ja) * 1997-02-04 1998-08-18 Yamanouchi Pharmaceut Co Ltd 新規なフェネタノール誘導体又はその塩
US6140342A (en) * 1998-09-17 2000-10-31 Pfizer Inc. Oxy substituted 4-carboxyamino-2-methyl-1,2,3,4-tetrahydroquinolines
GB9919713D0 (en) * 1999-08-19 1999-10-20 Queen Mary & Westfield College New medical use of high density lipoprotein
AUPQ429399A0 (en) * 1999-11-26 1999-12-23 Heart Research Institute, The Oxidized apolipoproteins and methods of use
AU777788B2 (en) * 1999-11-26 2004-10-28 Heart Research Institute Limited, The Oxidized apolipoproteins and methods of use

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CA2418238A1 (en) 2003-01-16
NO329848B1 (no) 2011-01-10
JP2004504355A (ja) 2004-02-12
IL154006A0 (en) 2003-07-31
ZA200300509B (en) 2004-02-17
NO20030137D0 (no) 2003-01-10
HU230151B1 (hu) 2015-09-28
NO20030137L (no) 2003-01-10
JP4928047B2 (ja) 2012-05-09
EP1303294A2 (de) 2003-04-23
DE10035352A1 (de) 2002-01-31
CA2418238C (en) 2012-06-05
WO2002007753A3 (de) 2003-02-13
KR100864079B1 (ko) 2008-10-16
KR20070108955A (ko) 2007-11-13
AU2001282004B2 (en) 2006-02-02
PL366395A1 (pl) 2005-01-24
HUP0300730A2 (hu) 2003-12-29
WO2002007753A2 (de) 2002-01-31
DK1303294T3 (da) 2006-10-30
DE50110552D1 (de) 2006-09-07
PL204406B1 (pl) 2010-01-29
IL154006A (en) 2010-05-31
US7053049B2 (en) 2006-05-30
ES2266234T3 (es) 2007-03-01
US20040014654A1 (en) 2004-01-22
NZ523784A (en) 2004-06-25
HUP0300730A3 (en) 2010-07-28
AU8200401A (en) 2002-02-05
ATE333887T1 (de) 2006-08-15
KR20030026980A (ko) 2003-04-03

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